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(1R,9R,10S)-4,17-Dimethyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2(7),3,5-triene

中文名称
——
中文别名
——
英文名称
(1R,9R,10S)-4,17-Dimethyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2(7),3,5-triene
英文别名
——
(1R,9R,10S)-4,17-Dimethyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2(7),3,5-triene化学式
CAS
——
化学式
C18H25N
mdl
——
分子量
255.4
InChiKey
KBEZZLAAKIIPFK-KBAYOESNSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3.8
  • 重原子数:
    19
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    3.2
  • 氢给体数:
    0
  • 氢受体数:
    1

文献信息

  • [EN] DEUTERATED MORPHINAN COMPOUNDS FOR USE IN TREATING AGITATION<br/>[FR] COMPOSÉS DE MORPHINANE DEUTÉRÉ POUR LE TRAITEMENT DE L'AGITATION
    申请人:CONCERT PHARMACEUTICALS INC
    公开号:WO2017020014A1
    公开(公告)日:2017-02-02
    This invention relates to methods of treating agitation comprising administering a morphinan compound or a pharmaceutically acceptable salt thereof. This invention also provides the use in methods of treating agitation and related disorders with such a morphinan compound in combination with quinidine, or pharmaceutically acceptable salt of either or both thereof.
    这项发明涉及治疗激动的方法,包括给予吗啡喃化合物或其药用可接受的盐。此发明还提供了在治疗激动和相关障碍的方法中使用这种吗啡喃化合物与奎尼丁或两者的药用可接受的盐的组合。
  • [EN] MORPHINAN COMPOUNDS<br/>[FR] COMPOSÉS DU MORPHINANE
    申请人:CONCERT PHARMACEUTICALS INC
    公开号:WO2010033801A1
    公开(公告)日:2010-03-25
    This invention relates to novel morphinan compounds and pharmaceutically acceptable salts thereof. This invention also provides compositions comprising a compound of this invention and the use of such compositions in methods of treating diseases and conditions that are beneficially treated by administering a σ1 receptor agonist that also has NMDA antagonist activity.
    本发明涉及新型的吗啡喃化合物及其可药用盐。本发明还提供了包含本发明化合物的组合物,以及在使用σ1受体激动剂且具有NMDA拮抗活性的药物治疗方法中使用该组合物来治疗疾病和状况。
  • Deuterated morphinane compounds
    申请人:Concert Pharmaceuticals Inc.
    公开号:EP2418211A1
    公开(公告)日:2012-02-15
    This invention relates to novel morphinan compounds and pharmaceutically acceptable salts thereof. This invention also provides compositions comprising a compound of this invention and the use of such compositions in methods of treating diseases and conditions that are beneficially treated by administering a a1 receptor agonist that also has NMDA antagonist activity.
    本发明涉及新型吗啡南化合物及其药学上可接受的盐类。本发明还提供了包含本发明化合物的组合物,以及这种组合物在治疗疾病和病症的方法中的用途,这些疾病和病症通过施用同时具有 NMDA 拮抗剂活性的 a1 受体激动剂而得到有益的治疗。
  • DEUTERATED MORPHINAN COMPOUNDS
    申请人:Concert Pharmaceuticals Inc.
    公开号:EP3248978A1
    公开(公告)日:2017-11-29
    This invention relates to novel morphinan compounds bearing a deuteromethyl substituent (CD3) and pharmaceutically acceptable salts thereof. This invention also provides compositions comprising a compound of this invention and the use of such compositions in methods of treating diseases and conditions that are beneficially treated by administering a σ1 receptor agonist that also has NMDA antagonist activity.
    本发明涉及含有氘代甲基取代基(CD3)的新型吗啡烷化合物及其药学上可接受的盐类。本发明还提供了包含本发明化合物的组合物,以及这种组合物在治疗疾病和病症的方法中的用途,这些疾病和病症通过施用同时具有 NMDA 拮抗剂活性的 σ1 受体激动剂而得到有益的治疗。
  • Morphinan compounds
    申请人:Concert Pharmaceuticals, Inc.
    公开号:US10022370B2
    公开(公告)日:2018-07-17
    This invention relates to novel morphinan compounds and pharmaceutically acceptable salts thereof. This invention also provides compositions comprising a compound of this invention and the use of such compositions in methods of treating diseases and conditions that are beneficially treated by administering a σ1 receptor agonist that also has NMDA antagonist activity.
    本发明涉及新型吗啡南化合物及其药学上可接受的盐类。本发明还提供了包含本发明化合物的组合物,以及这种组合物在治疗疾病和病症的方法中的用途,这些疾病和病症通过施用同时具有 NMDA 拮抗剂活性的 σ1 受体激动剂而得到有益的治疗。
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